Hanhart Syndrome: Introduction
Hanhart Syndrome: An autosomal recessive disorder due to a deficiency in the body of the tyrosine amino transferase enzyme.
More detailed information about the symptoms,
causes, and treatments of Hanhart Syndrome is available below.
Symptoms of Hanhart Syndrome
See full list of 9
symptoms of Hanhart Syndrome
Wrongly Diagnosed with Hanhart Syndrome?
Hanhart Syndrome: Complications
Read more about complications of Hanhart Syndrome.
Causes of Hanhart Syndrome
Read more about causes of Hanhart Syndrome.
Disease Topics Related To Hanhart Syndrome
Research the causes of these diseases that are similar to, or related to, Hanhart Syndrome:
Misdiagnosis and Hanhart Syndrome
Leg cramps at night a classic sign: The symptom of having leg muscle cramps,
particularly at night, is a classic sign of undiagnosed diabetes.
However, there are also...read more »
Psoriasis often undiagnosed cause of skin symptoms in children: Children who suffer
from the skin disorder called psoriasis can often go undiagnosed.
The main problem is that psoriasis is rare in children,...read more »
Read more about Misdiagnosis and Hanhart Syndrome
Hanhart Syndrome: Research Doctors & Specialists
Research related physicians and medical specialists:
- Ear, Nose & Throat Specialists:
- Skin Health Specialists (Dermatology):
- Arthritis & Joint Health Specialists (Rheumatology):
- more specialists...»
Other doctor, physician and specialist research services:
Hanhart Syndrome: Animations
More Hanhart Syndrome animations & videos
Statistics for Hanhart Syndrome
Hanhart Syndrome: Broader Related Topics
Types of Hanhart Syndrome
User Interactive Forums
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Definitions of Hanhart Syndrome:
Hanhart Syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Hanhart Syndrome, or a subtype of Hanhart Syndrome,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Hanhart Syndrome as a "rare disease".
Source - Orphanet
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